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新型药物递释系统改善角膜炎治疗

Novel Drug Delivery Systems to Improve the Treatment of Keratitis.

机构信息

Department of Pharmaceutical Technology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey.

Department of Pharmaceutical Technology, Faculty of Pharmacy, Erzincan Binali Yıldırım University, Erzincan, Turkey.

出版信息

J Ocul Pharmacol Ther. 2022 Jul-Aug;38(6):376-395. doi: 10.1089/jop.2021.0127. Epub 2022 Jun 28.

Abstract

Keratitis is a disease characterized by inflammation of the cornea caused by different pathogens. It can cause serious visual morbidity if not treated quickly. Depending on the pathogen causing keratitis, eye drops containing antibacterial, antifungal, or antiviral agents such as besiloxacin, moxifloxacin, ofloxacin, voriconazol, econazole, fluconazole, and acyclovir are used, and these drops need to be applied frequently due to their low bioavailability. Studies are carried out on formulations with extended residence time in the cornea and increased permeability. These formulations include various new drug delivery systems such as inserts, nanoparticles, liposomes, niosomes, cubosomes, microemulsions, gels, contact lenses, nanostructured lipid carriers, carbon quantum dots, and microneedles. and studies with these formulations have shown that the residence time of the active substances in the cornea is prolonged, and their ocular bioavailability is increased. In addition, studies have shown that these formulations successfully treat keratitis. However, it has been observed that fluoroquinolones are used in most of the studies; similar drug delivery systems are generally preferred for antifungal drugs, and studies for viral and acanthameba keratitis are limited. There is a need for new studies on different types of keratitis and different drug active substances. At the same time, proving the efficacy of drug delivery systems, which give promising results in animal models, with clinical studies is of great importance for progress in the treatment of keratitis.

摘要

角膜炎是一种由不同病原体引起的角膜炎症疾病。如果不及时治疗,可能会导致严重的视力障碍。根据引起角膜炎的病原体,使用含有抗菌、抗真菌或抗病毒药物的眼药水,如贝西沙星、莫西沙星、氧氟沙星、伏立康唑、益康唑、氟康唑和阿昔洛韦等,由于这些药物的生物利用度较低,因此需要频繁滴用。目前正在研究延长在角膜中的停留时间和增加通透性的制剂。这些制剂包括各种新的药物传递系统,如插入物、纳米颗粒、脂质体、尼莫司汀、立方脂质体、微乳液、凝胶、隐形眼镜、纳米结构脂质载体、碳量子点和微针。这些制剂的研究表明,活性物质在角膜中的停留时间延长,其眼部生物利用度增加。此外,研究表明这些制剂成功地治疗了角膜炎。然而,人们观察到,在大多数研究中都使用了氟喹诺酮类药物;一般来说,相似的药物传递系统更适合抗真菌药物,而针对病毒性和棘阿米巴性角膜炎的研究则有限。需要对不同类型的角膜炎和不同的药物活性物质进行新的研究。同时,通过临床研究证明在动物模型中给出有希望结果的药物传递系统的疗效,对于角膜炎治疗的进展非常重要。

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